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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567160Generated: October 31, 2026

Oxalyl chloride → Ethyl 7-(4-chlorophenyl)-7-oxoheptanoate

https://huagongshe.com/reaction/567160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantEthyl hydrogen heptane-1,7-dioateHCID 118383—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 7-(4-chlorophenyl)-7-oxoheptanoateHCID 11065929196.8%

Reaction Steps

N,N-dimethylformamide(1 drop) was added to a tetrahydrofuran solution(40 ml) of pimelic acid monoethyl ester(25.5 g), and thereto oxalyl chloride(18.8 g) was added dropwise. After stirring for 2 hours at room temperature, the reaction mixture was concentrated. The residue was added dropwise to a mixture of chlorobenzene(61.0 g) and aluminum chloride anhydrous (36.1 g) under ice water. After stirring for 3 hours, the reaction mixture was poured into 1N-hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, and dried(MgSO4). The solvent was evaporated to give ethyl 6-(4-chlorobenzoyl)hexanate (37.7 g, 97%) as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177452B1
Source datasetuspto-grants-2001_01
ORD IDord-8e032c037879423db8794974e07bf39a
Source noteuspto-grants-2001_01